Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57515868 | HCID 57515868 | — |
| Solvent | Tetrahydrofuran 2-propanol | HCID 22597222 | — |
| Product | HCID 57515869 | HCID 57515869 | — |
Reaction Steps
A mixture of 1-(5-(methoxymethoxy)-2-(trifluoromethyl)pyridin-4-yl)ethanone (3.2 g, 13 mmol) and 5N HCl (40 ml) in i-PrOH/THF (1:1, 40 ml) was stirred at 45° C. overnight. The mixture was cooled, concentrated, taken up in H2O, neutralized with saturated NaHCO3, and extracted with DCM (3×). The organic layers were combined, dried over Na2SO4, and concentrated to give the title compound as a tan solid. MS (m+1): 206.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173810B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-6ceadbf718b84f8480699e29a62cd13b |
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| Source note | uspto-grants-2012_05 |
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